Paragraph 19 Medicated feedingstuff prescriptions for feedingstuffs containing a medicinal premixF13F14E1

the name and address of the person prescribing the product;

the qualifications enabling the person to prescribe the product;

the name and address of the keeper of the animals to be treated;

the species of animal, identification and number of the animals;

the premises at which the animals are kept if this is different from the address of the keeper;

the diagnosed disease to be treated or prevented (in the case of immunological veterinary medicinal products or antiparasitics without antimicrobial effects);

the date of the prescription;

the signature or other authentication of the person prescribing the product;

the name, active substance, amount of the product prescribed and inclusion rate of the medicinal premix and resulting inclusion rate of the active substance;

the dosage and administration instructions;

any necessary warnings;

a statement that the prescription may not be re-used;

the withdrawal period;

the manufacturer or the distributor of the feedingstuffs (who must be F6authorised for the purpose) F7, whichever is the supplier to the end user;

if the validity exceeds one month, a statement that not more than 31 days’ supply may be provided at any time;

the name, type and quantity of feedingstuffs to be used;

the overall amount of feedingstuff to be supplied under the prescription;

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

any special instructions;

the percentage of the prescribed feedingstuffs to be added to the daily ration; and

if it is prescribed under the cascade, a statement to that effect.